Issue 30, 2018

Metathesis cleavage of an N[double bond, length as m-dash]N bond in benzo[c]cinnolines and azobenzenes by triply-bonded ditungsten complexes

Abstract

A metathesis reaction of a W[triple bond, length as m-dash]W bond and an N[double bond, length as m-dash]N bond was observed by reacting a W–W triply-bonded W(III)2 complex, (tBuO)3W[triple bond, length as m-dash]W(OtBu)3 (1), with benzo[c]cinnoline derivatives to form biphenyl-linked dinuclear (imido)tungsten complexes 2–4. When azobenzene was used as the substrate, a trans to cis isomerization induced by blue-LED light was essential prior to the metathesis cleavage of the N[double bond, length as m-dash]N bond by the W[triple bond, length as m-dash]W bond of (Me2N)2(TfO)W[triple bond, length as m-dash]W(OTf)(NMe2)2 (6), affording the corresponding imido-bridged dinuclear tungsten complexes 7–9.

Graphical abstract: Metathesis cleavage of an N [[double bond, length as m-dash]] N bond in benzo[c]cinnolines and azobenzenes by triply-bonded ditungsten complexes

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2017
Accepted
07 Feb 2018
First published
08 Feb 2018

Chem. Commun., 2018,54, 3709-3711

Metathesis cleavage of an N[double bond, length as m-dash]N bond in benzo[c]cinnolines and azobenzenes by triply-bonded ditungsten complexes

H. Ikeda, K. Nishi, H. Tsurugi and K. Mashima, Chem. Commun., 2018, 54, 3709 DOI: 10.1039/C7CC08570B

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